Indigenome VS ClinVar IDs Relevant information available in ClinVar
Variant Identifiers ClinVar Name Variant Type Clinical Significance Phenotype Condition Review Status Variation/condition record
IndiGenomes: chr2:43851647:C>A
 
ClinVar:           chr2:43851647:C>A 		NM_022437.3(ABCG8):c.386C>A (p.Ser129Ter) SNV
Pathogenic Condition: not provided Criteria Provided
Single Submitter

1 SubmittersRCV003109206